Lignans isolated from flower buds of Magnolia fargesii attenuate airway inflammation induced by cigarette smoke in vitro and in vivo

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dc.contributor.authorSu Ui Lee-
dc.contributor.authorHyung Won Ryu-
dc.contributor.authorSeoghyun Lee-
dc.contributor.authorI S Shin-
dc.contributor.authorJi Hee Choi-
dc.contributor.authorJae Won Lee-
dc.contributor.authorJinhyuk Lee-
dc.contributor.authorMun-Ock Kim-
dc.contributor.authorHyun-Jun Lee-
dc.contributor.authorKyung Seop Ahn-
dc.contributor.authorS T Hong-
dc.contributor.authorSei-Ryang Oh-
dc.date.accessioned2018-10-24T16:30:34Z-
dc.date.available2018-10-24T16:30:34Z-
dc.date.issued2018-
dc.identifier.issn1663-9812-
dc.identifier.uri10.3389/fphar.2018.00970ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/18082-
dc.description.abstractThe flower buds of Magnolia fargesii, known traditionally as Xinyi, exert anti-inflammatory effects against inflammatory lung diseases such as COPD. Lignans isolated from Xinyi are an important group of plant-derived anti-inflammatory compounds. However, the mechanisms of action underlying their protective effects against COPD are not yet fully understood. Here, we showed that seven lignans (lignans 1-7) obtained from a CHCl3 fraction of Xinyi effectively suppress the inflammatory response in CSC-stimulated airway epithelial cells (in vitro) and in a mouse model of COPD established by exposure to CS and LPS. The CHCl3 fraction was found to inhibit CSC-induced IL-6 expression in human airway epithelial cells and to suppress the infiltration of inflammatory cells (neutrophils and macrophages) and secretion of inflammatory cytokines, such as tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) in the mouse model. Similarly, each of the seven lignans isolated from the CHCl3 fraction also suppressed the infiltration of inflammatory cells (neutrophils and macrophages) and secretion of inflammatory mediators such as reactive oxygen species (ROS), TNF-α, and IL-6 in vivo. Notably, all lignan compounds significantly suppressed both extracellular signal-related kinase (ERK) and Akt phosphorylation levels in CSC-stimulated human lung mucoepidermoid carcinoma (NCI-H292) cells. Of these, lignan 1 (dimethylpinoresinol) inhibited the expression of CSC-induced inflammatory cytokines (IL-1β, -6, and -8) in vitro in a dose-dependent manner by suppressing the activation of epidermal growth factor receptor (EGFR) and its downstream effectors, including ERK and Akt, in NCI-H292 cells. Our results show that the lignans isolated from Xinyi may prevent airway inflammatory diseases through the suppression of EGFR and its downstream effectors.-
dc.publisherFrontiers Media Sa-
dc.titleLignans isolated from flower buds of Magnolia fargesii attenuate airway inflammation induced by cigarette smoke in vitro and in vivo-
dc.title.alternativeLignans isolated from flower buds of Magnolia fargesii attenuate airway inflammation induced by cigarette smoke in vitro and in vivo-
dc.typeArticle-
dc.citation.titleFrontiers in Pharmacology-
dc.citation.number0-
dc.citation.endPage970-
dc.citation.startPage970-
dc.citation.volume9-
dc.contributor.affiliatedAuthorSu Ui Lee-
dc.contributor.affiliatedAuthorHyung Won Ryu-
dc.contributor.affiliatedAuthorSeoghyun Lee-
dc.contributor.affiliatedAuthorJi Hee Choi-
dc.contributor.affiliatedAuthorJae Won Lee-
dc.contributor.affiliatedAuthorJinhyuk Lee-
dc.contributor.affiliatedAuthorMun-Ock Kim-
dc.contributor.affiliatedAuthorHyun-Jun Lee-
dc.contributor.affiliatedAuthorKyung Seop Ahn-
dc.contributor.affiliatedAuthorSei-Ryang Oh-
dc.contributor.alternativeName이수의-
dc.contributor.alternativeName류형원-
dc.contributor.alternativeName이석현-
dc.contributor.alternativeName신인식-
dc.contributor.alternativeName최지희-
dc.contributor.alternativeName이재원-
dc.contributor.alternativeName이진혁-
dc.contributor.alternativeName김문옥-
dc.contributor.alternativeName이현준-
dc.contributor.alternativeName안경섭-
dc.contributor.alternativeName홍성태-
dc.contributor.alternativeName오세량-
dc.identifier.bibliographicCitationFrontiers in Pharmacology, vol. 9, pp. 970-970-
dc.identifier.doi10.3389/fphar.2018.00970-
dc.subject.keywordAkt-
dc.subject.keywordCOPD-
dc.subject.keywordCS-
dc.subject.keywordEGFR-
dc.subject.keywordERK-
dc.subject.keywordMagnolia fargesii-
dc.subject.keywordlignans-
dc.subject.localAKT-
dc.subject.localAkt-
dc.subject.localCOPD-
dc.subject.localCS-
dc.subject.localEGFR-
dc.subject.localERK-
dc.subject.localErk-
dc.subject.localMagnolia fargesii-
dc.subject.localmagnolia fargesii-
dc.subject.locallignan-
dc.subject.localLignans-
dc.subject.localLignan-
dc.subject.locallignans-
dc.description.journalClassY-
Appears in Collections:
Center for Gene & Cell Theraphy > 1. Journal Articles
Ochang Branch Institute > Natural Product Research Center > 1. Journal Articles
Synthetic Biology and Bioengineering Research Institute > Genome Editing Research Center > 1. Journal Articles
Ochang Branch Institute > 1. Journal Articles
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